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Distinct neuropeptide-receptor modules regulate a sex-specific behavioral response to a pheromone
Dioecious species are a hallmark of the animal kingdom, with opposing sexes responding differently to identical sensory cues. Here, we study the response of C. elegans to the small-molecule pheromone, ascr#8, which elicits opposing behavioral valences in each sex. We identify a novel neuropeptide-ne...
Autores principales: | , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group UK
2021
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8408276/ https://www.ncbi.nlm.nih.gov/pubmed/34465863 http://dx.doi.org/10.1038/s42003-021-02547-7 |
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author | Reilly, Douglas K. McGlame, Emily J. Vandewyer, Elke Robidoux, Annalise N. Muirhead, Caroline S. Northcott, Haylea T. Joyce, William Alkema, Mark J. Gegear, Robert J. Beets, Isabel Srinivasan, Jagan |
author_facet | Reilly, Douglas K. McGlame, Emily J. Vandewyer, Elke Robidoux, Annalise N. Muirhead, Caroline S. Northcott, Haylea T. Joyce, William Alkema, Mark J. Gegear, Robert J. Beets, Isabel Srinivasan, Jagan |
author_sort | Reilly, Douglas K. |
collection | PubMed |
description | Dioecious species are a hallmark of the animal kingdom, with opposing sexes responding differently to identical sensory cues. Here, we study the response of C. elegans to the small-molecule pheromone, ascr#8, which elicits opposing behavioral valences in each sex. We identify a novel neuropeptide-neuropeptide receptor (NP/NPR) module that is active in males, but not in hermaphrodites. Using a novel paradigm of neuropeptide rescue that we established, we leverage bacterial expression of individual peptides to rescue the sex-specific response to ascr#8. Concurrent biochemical studies confirmed individual FLP-3 peptides differentially activate two divergent receptors, NPR-10 and FRPR-16. Interestingly, the two of the peptides that rescued behavior in our feeding paradigm are related through a conserved threonine, suggesting that a specific NP/NPR combination sets a male state, driving the correct behavioral valence of the ascr#8 response. Receptor expression within pre-motor neurons reveals novel coordination of male-specific and core locomotory circuitries. |
format | Online Article Text |
id | pubmed-8408276 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | Nature Publishing Group UK |
record_format | MEDLINE/PubMed |
spelling | pubmed-84082762021-09-22 Distinct neuropeptide-receptor modules regulate a sex-specific behavioral response to a pheromone Reilly, Douglas K. McGlame, Emily J. Vandewyer, Elke Robidoux, Annalise N. Muirhead, Caroline S. Northcott, Haylea T. Joyce, William Alkema, Mark J. Gegear, Robert J. Beets, Isabel Srinivasan, Jagan Commun Biol Article Dioecious species are a hallmark of the animal kingdom, with opposing sexes responding differently to identical sensory cues. Here, we study the response of C. elegans to the small-molecule pheromone, ascr#8, which elicits opposing behavioral valences in each sex. We identify a novel neuropeptide-neuropeptide receptor (NP/NPR) module that is active in males, but not in hermaphrodites. Using a novel paradigm of neuropeptide rescue that we established, we leverage bacterial expression of individual peptides to rescue the sex-specific response to ascr#8. Concurrent biochemical studies confirmed individual FLP-3 peptides differentially activate two divergent receptors, NPR-10 and FRPR-16. Interestingly, the two of the peptides that rescued behavior in our feeding paradigm are related through a conserved threonine, suggesting that a specific NP/NPR combination sets a male state, driving the correct behavioral valence of the ascr#8 response. Receptor expression within pre-motor neurons reveals novel coordination of male-specific and core locomotory circuitries. Nature Publishing Group UK 2021-08-31 /pmc/articles/PMC8408276/ /pubmed/34465863 http://dx.doi.org/10.1038/s42003-021-02547-7 Text en © The Author(s) 2021 https://creativecommons.org/licenses/by/4.0/Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) . |
spellingShingle | Article Reilly, Douglas K. McGlame, Emily J. Vandewyer, Elke Robidoux, Annalise N. Muirhead, Caroline S. Northcott, Haylea T. Joyce, William Alkema, Mark J. Gegear, Robert J. Beets, Isabel Srinivasan, Jagan Distinct neuropeptide-receptor modules regulate a sex-specific behavioral response to a pheromone |
title | Distinct neuropeptide-receptor modules regulate a sex-specific behavioral response to a pheromone |
title_full | Distinct neuropeptide-receptor modules regulate a sex-specific behavioral response to a pheromone |
title_fullStr | Distinct neuropeptide-receptor modules regulate a sex-specific behavioral response to a pheromone |
title_full_unstemmed | Distinct neuropeptide-receptor modules regulate a sex-specific behavioral response to a pheromone |
title_short | Distinct neuropeptide-receptor modules regulate a sex-specific behavioral response to a pheromone |
title_sort | distinct neuropeptide-receptor modules regulate a sex-specific behavioral response to a pheromone |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8408276/ https://www.ncbi.nlm.nih.gov/pubmed/34465863 http://dx.doi.org/10.1038/s42003-021-02547-7 |
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